Expression of macrophage migration inhibitory factor during Pseudomonas keratitis

Authors: Thakur, Archana1; Xue, Mei Lang1; Wang, Wen1; Lloyd, Andrew2; Wakefield, Denis2; Willcox, Mark DP1

Source: Clinical & Experimental Ophthalmology, Volume 29, Number 3, June 2001 , pp. 179-182(4)

Publisher: Blackwell Publishing

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Abstract:

Macrophage migration inhibitory factor (MIF) is a recently rediscovered pro-inflammatory cytokine, and has been shown to play a role in the regulation of neutrophil chemokines and angiogenesis. Corneal epithelial and endothelial cells have been shown to express MIF. This study evaluated the expression of MIF during Pseudomonas keratitis in mice and in vitro using a corneal epithelial cell line. Three strains of P. aeruginosa, 6294 (invasive strain), 6206 (cytotoxic strain) and Paer1 (non- infectious strain) were used. Both cytotoxic and invasive strains were isolated from human corneal ulcers and the Paer1 strain was isolated from a non-infectious condition. Following challenge in mouse corneas or a corneal epithelial cell line, corneal homogenates or lysed corneal epithelial cells were used to isolate RNA. Migration inhibitory factor mRNA expression in the mouse cornea or human corneal epithelial cells was examined by reverse transcription-polymerase chain reaction analysis, and was found to be expressed as early as 4 h after the injury (scratch controls) or infection in the mouse corneas. Migration inhibitory factor mRNA in scratch controls and Paer1-inoculated corneas showed peak levels at 4 h post-challenge and this dropped by 24 h post-challenge. Corneas challenged with invasive and cytotoxic strains showed peak expression 24 h post-challenge. Migration inhibitory factor mRNA levels were significantly higher in invasive and cytotoxic strain inoculated corneas compared to Paer1 inoculated corneas. Challenging the corneal epithelial cell line with Pseudomonas 6294 and 6206 strains induced peak expression at 8 h and levels were decreased by 12 h. Epithelial cells inoculated with recombinant human interleukin-1β protein induced very high levels of MIF mRNA at all time points compared to infected and control corneal epithelial cells. High expression of MIF in the infected corneas suggests that it may have a role in the pathogenesis of corneal disease induced by invasive and cytotoxic strains of P. aeruginosa.

Keywords: cornea; cytokine; keratitis; macrophage migration inhibitory factor; Pseudomonas aeruginosa

Document Type: Research article

DOI: 10.1046/j.1442-9071.2001.00405.x

Affiliations: 1: Cooperative Research Centre For Eye Research and Technology, and 2: School of Pathology, Inflammation Research Unit, The University of New South Wales, Sydney, New South Wales, Australia

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